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on page 4 showing 20 out of 620,309 results

Cite this (MGI Cat# 5618136, RRID:MGI:5618136)

Source Database: MGI, catalog # 5618136
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * FVB/N
Affected Genes: Casp8, Ikbkg
Genomic Alteration: tm1Clie; tm1.1Chtr; Tg(Alb1-cre)7Gsc
Availability: Availability unknown check source stock center
Reference: PMID:21878202
Notes: increased bile salt level, decreased body size, increased circulating alkaline phosphatase level, abnormal liver morphology, liver fibrosis, abnormal circulating enzyme level, abnormal biliary tract morphology, enlarged liver, intrahepatic cholestasis, neoplasm, increased circulating bilirubin level, hepatic necrosis Allele Detail: Transgenic, Targeted

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Cite this (IMSR Cat# CMMR:519D12, RRID:IMSR_CMMR:519D12)

Source Database: IMSR, catalog # CMMR:519D12
Genetic Background:
Affected Genes: Etv5
Genomic Alteration: Gt (519D12) Cmhd
Availability: mouse cells
Reference:
Notes: gene symbol note: ets variant 5; unclassified: gene trap 519D12, Centre for Modeling Human Disease

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Cite this (IMSR Cat# TIGM:IST14061E6, RRID:IMSR_TIGM:IST14061E6)

Source Database: IMSR, catalog # TIGM:IST14061E6
Genetic Background:
Affected Genes: Gnb1
Genomic Alteration: Gt(IST14061E6)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: guanine nucleotide binding protein (G protein), beta 1; unclassified: gene trap IST14061E6, Texas A&M Institute for Genomic Medicine

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Cite this (IMSR Cat# TIGM:IST14142D10, RRID:IMSR_TIGM:IST14142D10)

Source Database: IMSR, catalog # TIGM:IST14142D10
Genetic Background:
Affected Genes: Ccpg1
Genomic Alteration: Gt(IST14142D10)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: cell cycle progression 1; unclassified:

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Cite this (IMSR Cat# RBRC10220, RRID:IMSR_RBRC10220)

Source Database: IMSR, catalog # RBRC10220
Genetic Background:
Affected Genes: Ripk3, Rnf31
Genomic Alteration: em2Kiwa, tm1.1Kiwa
Availability: live mouse
Reference:
Notes: gene symbol note: receptor-interacting serine-threonine kinase 3, ring finger protein 31; mutant stock: endonuclease-mediated mutation 2, Kazuhiro Iwai, targeted mutation 1.1, Kazuhiro Iwai

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Cite this (MMRRC Cat# 049405-UCD, RRID:MMRRC_049405-UCD)

Source Database: MMRRC, catalog # 049405-UCD
Genetic Background: Deletion
Affected Genes: Recql4
Genomic Alteration:
Availability:
Reference:
Notes: Mutation type: Deletion

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Cite this (IMSR Cat# RBRC-AES1481, RRID:IMSR_RBRC-AES1481)

Source Database: IMSR, catalog # RBRC-AES1481
Genetic Background:
Affected Genes: Sox13
Genomic Alteration: Gt(37v-355)Yais
Availability: mouse cells
Reference:
Notes: gene symbol note: SRY (sex determining region Y)-box 13; unclassified: gene trap 37v-355, Yasumasa Ishida

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Cite this (FlyBase Cat# FBst1017855, RRID:FlyBase_FBst1017855)

Source Database: FlyBase, catalog # FBst1017855
Genetic Background:
Affected Genes:
Genomic Alteration: PBac{WH}f02593
Availability: Availability unknown check source stock centers
Reference:
Notes:

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Cite this (BDSC Cat# 69340, RRID:BDSC_69340)

Source Database: BDSC, catalog # 69340
Genetic Background:
Affected Genes: Scer\GAL4,Scr,w
Genomic Alteration: Chromosome/1;3, breakpoints/68A4, 3L:11070538..11070538 (r6, Ti)
Availability: Available
Reference:
Notes: Expresses the DNA binding domain of GAL4 under control of sequences in/near Scr (FBgn0003339). May be segregating TM3, Sb[1] Ser[1].

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Cite this (MMRRC Cat# 041136-MU, RRID:MMRRC_041136-MU)

Source Database: MMRRC, catalog # 041136-MU
Genetic Background: Chemically Induced
Affected Genes: 4932438A13Rik, Adprhl1, Atp10d, Bcdin3d, Col11a1, Cp, Dnah17, Dpp4, Dusp6, Exoc1, Fbxl13, Gm12992, Gpsm1, Gstm4, Hectd4, Izumo3, Kcna4, Lrrc10, Madd, Mcpt4, Mrgprx3-ps, Mrm1, Nav2, Noct, Ntn1, Olfr417, Plekhg3, Ppp2r1a, Rhbdl2, Slc10a1, Sohlh2, Srrm2, Syn3, Taf5, Tas2r136, Tex45, Tnk2, Ttn, Ubxn6, Usp7, Vmn1r115, Vmn2r50, Vmn2r58, Vmn2r86, Vmn2r99, Zfp462
Genomic Alteration:
Availability:
Reference:
Notes: Mutation type: Chemically Induced

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Cite this (FlyBase Cat# FBst0451624, RRID:FlyBase_FBst0451624)

Source Database: FlyBase, catalog # FBst0451624
Genetic Background:
Affected Genes:
Genomic Alteration:
Availability: Availability unknown check source stock centers
Reference:
Notes:

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Cite this (MGI Cat# 3699598, RRID:MGI:3699598)

Source Database: MGI, catalog # 3699598
Genetic Background: involves: C3HeB/FeJ * C57BL/6J
Affected Genes: Sox10, Sox10m3
Genomic Alteration: C3HeB/FeJ; Dom; C57BL/6J
Availability: Availability unknown check source stock center
Reference: PMID:15843399
Notes: aganglionic megacolon Allele Detail: QTL, Spontaneous

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Cite this (ZFIN Cat# ZDB-GENO-040824-4, RRID:ZFIN_ZDB-GENO-040824-4)

Source Database: ZFIN, catalog # ZDB-GENO-040824-4
Genetic Background: unspecified
Affected Genes: cct5
Genomic Alteration: hi2972bTg
Availability:
Reference:
Notes: ZFIN prefers authors to cite using the other (ZDB-ALT-prefixed) identifier.

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Cite this (BDSC Cat# 63666, RRID:BDSC_63666)

Source Database: BDSC, catalog # 63666
Genetic Background:
Affected Genes: DMAP1,Scer\UAS,v,y
Genomic Alteration: Chromosome/1;2, breakpoints/25C6, 2L:5108448..5108448 (r6, Ti)
Availability: Available
Reference:
Notes: Expresses dsRNA for RNAi of DMAP1 (FBgn0034537) under UAS control. May be segregating CyO.

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Cite this (MMRRC Cat# 036018-MU, RRID:MMRRC_036018-MU)

Source Database: MMRRC, catalog # 036018-MU
Genetic Background: Transgene
Affected Genes: cre/ERT2
Genomic Alteration:
Availability:
Reference:
Notes: Research areas: Research Tools; Mutation type: Transgene

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Cite this (FlyBase Cat# FBst0468029, RRID:FlyBase_FBst0468029)

Source Database: FlyBase, catalog # FBst0468029
Genetic Background:
Affected Genes:
Genomic Alteration:
Availability: Availability unknown check source stock centers
Reference:
Notes:

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Cite this (IMSR Cat# TIGM:IST14413D9, RRID:IMSR_TIGM:IST14413D9)

Source Database: IMSR, catalog # TIGM:IST14413D9
Genetic Background:
Affected Genes: Dnajc16
Genomic Alteration: Gt(IST14413D9)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: DnaJ heat shock protein family (Hsp40) member C16; unclassified: gene trap IST14413D9, Texas A&M Institute for Genomic Medicine

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Cite this (MGI Cat# 5294945, RRID:MGI:5294945)

Source Database: MGI, catalog # 5294945
Genetic Background: involves: FVB/N
Affected Genes:
Genomic Alteration: Tg(CAG-NRIP1)51Row
Availability: Availability unknown check source stock center
Reference: PMID:20083575
Notes: ascites, pulmonary vascular congestion, cardiomyopathy, pulmonary fibrosis, premature death, pregnancy-related premature death, pleural effusion, decreased mitochondria number, lung inflammation, enlarged heart atrium, decreased cardiac muscle contractility, congestive heart failure, cardiac interstitial fibrosis, cardiac hypertrophy, abnormal respiratory electron transport chain, abnormal heart atrium morphology, abnormal heart ventricle morphology, abnormal mitochondrion morphology, abnormal myocardial fiber morphology, abnormal atrial thrombosis Allele Detail: Transgenic

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Cite this (MGI Cat# 3640618, RRID:MGI:3640618)

Source Database: MGI, catalog # 3640618
Genetic Background: involves: 129 * C57BL/6J * FVB
Affected Genes: Lepr
Genomic Alteration: Tg(Pomc1-cre)16Lowl; tm1.1Chua
Availability: Availability unknown check source stock center
Reference: PMID:15207242, PMID:16423694
Notes: abnormal mesenteric fat pad morphology, increased circulating leptin level, obese, abnormal renal fat pad morphology, abnormal epididymal fat pad morphology, increased total body fat amount, abnormal fat pad morphology, abnormal gonadal fat pad morphology, abnormal fat pad morphology, increased circulating leptin level, abnormal mesenteric fat pad morphology, increased body weight, increased total body fat amount, abnormal renal fat pad morphology Allele Detail: Transgenic, Targeted

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Cite this (IMSR Cat# KOMP:CSD23680-1a-Wtsi, RRID:IMSR_KOMP:CSD23680-1a-Wtsi)

Source Database: IMSR, catalog # KOMP:CSD23680-1a-Wtsi
Genetic Background:
Affected Genes: Cd300lg
Genomic Alteration: tm1a(KOMP)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: CD300 molecule like family member G; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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